Eye Problems, Hearing Loss May Be Linked
... were offered genetic testing for mutations in the gjb2
gene. Of the 144 who had the screening, 27 (18.8 percent) had two mutated copies of the gjb2
gene, and one of the 27 (3.7 percent) had an eye d...s.
"This is consistent with the impression that gjb2
mutations result in sensorineural hearing loss but...
Oragene and DNA sequencing with ABI PRISM
2. Sugata, A. et al. (2002). High-throughput screening for gjb2
its clinical application to genetic testing in prelingual deafness screening
mutations. Auris, Nasus, Larynx. 29: 231-239.
3. Elit, L., Jack, ...
GJB2 - Wikipedia, the free encyclopediaGJB2
, is a human gene encoding for Gap junction protein, beta 2, 26kDa, or Connexin 26. Defects in this gene lead to the most common form of congenital deafness in developed countries, called DFNB1, also known as Connexin 26 deafness or GJB2
GJB2 - gap junction protein, beta 2, 26kDa - Genetics Home Reference
nonsyndromic deafness - caused by mutations in the GJB2
gene ... GJB2
mutations probably alter gap junctions, which may disturb the level of ...
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
Complete information for GJB2
gene (protein-coding), gap junction protein, beta 2, 26kDa ... GJB2
Gene in genomic location: bands according to Ensembl, ...
GJB2 definition - Medical Dictionary definitions of popular medical ...
Online Medical Dictionary and glossary with medical definitions ... The GJB2
gene is a member of the gap junction or connexin family. ...
Gjb2 MGI Mouse Gene Detail - MGI:95720 - gap junction protein, beta 2
Chr14:57717455-57723502 bp, - strand has data for genome coordinates, ... Comparative Map (Mouse/Human Gjb2
± 2 cM) TreeFam: TF329606. Sequences ...
GJB2 antibody (ab59020) | Abcam
Goat polyclonal to GJB2
. Gap junction channels consist of connexin protein ... Mutations in GJB2
are associated with genetically derived hearing impairments, ...